Devices not Drugs: How rethinking patient care could help save the NHS with Michael Branagan-Harris
Description
EP 346 - We chat with the founder & CEO of Device Access - who help MedTech companies gain market access and regulatory approval - about how over regulation can stifle innovation and lead to an adverse impact on patient care and outcomes.
Michael Branigan tells us about:
Why US companies aren’t interested infringing their devices to the UK anymore (hint it’s cos we are tiny)
Why regulation is stifling innovation, and how that is bad for all of us, but particularly the NHS
He also mentions Brexit, but not for the reasons that you’d expect.
Chapters:
00:00 BWB with Michael Branagan-Harris
01:51 The Changing Landscape UK MedTech
02:46 Impact of European Medical Device Regulations
04:46 Challenges in the MedTech Industry
05:55 Gov Initiatives and Their Shortcomings
07:28 Understanding Medical Device Regulations
14:42 The Role of NICE and Market Access
28:56 The Future of MedTech and Market Strategies
35:22 Affordability vs. Innovation in Healthcare
37:00 Challenges in Medtech vs. Pharma
37:39 Navigating the NHS Procurement Process
38:59 Leveraging Data for Healthcare Solutions
41:53 Global Perspectives on Healthcare Systems
49:20 The Role of MedTech in Modern Healthcare
52:12 Independent Clinical Evidence
55:34 Quick Fire Round - Get to Know Michael
01:00:06 Wrap Up and Advice for Entrepreneurs
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